Suppr超能文献

使用部分T细胞清除且不进行移植后移植物抗宿主病预防的非恶性疾病安全有效的异基因骨髓移植。

Safe and efficacious allogeneic bone marrow transplantation for nonmalignant disorders using partial T cell depletion and no posttransplantation graft-versus-host-disease prophylaxis.

作者信息

Elhasid Ronit, Arush Myriam Ben, Zaidman Irena, Leiba Ronit, Barak Ayelet Ben, Postovsky Sergey, Haddad Nuhad, Katz Tami, Pollack Shimon, Sami Ivanka, Gidoni Osnat, Rubin Dina, Mandel Hanna, Attias Dina, Reisner Yair, Etzioni Amos, Rowe Jacob M

机构信息

Department of Pediatric Hemato-Oncology, Meyer Children Hospital, Haifa, Israel.

出版信息

Biol Blood Marrow Transplant. 2007 Mar;13(3):329-38. doi: 10.1016/j.bbmt.2006.10.028.

Abstract

In an attempt to abrogate the deleterious effects of graft-versus-host disease (GVHD), allogeneic transplantation for nonmalignant diseases was performed using high-dose CD34-cell infusion, partial T cell depletion, and no posttransplantation GVHD prophylaxis. Between 1998 and 2004, 16 patients with matched related donors were treated. Median age was 1.5 years (range, 5 months-18 years). The conditioning regimen consisted of busulphan 16 mg/kg, cyclophosphamide 200 mg/kg, antithymocyte globulin (ATG) 25 mg/kg, and fludarabine 200 mg/m(2). No GVHD prophylaxis was given. High doses of CD34 cells, positively selected by immunomagnetic beads, were infused at a median dose of 10.7 x 10(6) CD34/kg (range, 7.4-50 x 10(6)). A total of 1 x 10(5)/kg T cells were given. All patients engrafted, with no graft rejections. All were alive and well at a median of 37 months posttransplantation (range, 18-89 months). Only 1 patient developed chronic GVHD. No episodes of severe infection occurred during or after transplantation. Immunologic reconstitution with CD3/CD4 T cells > 200/microL was observed at a median of 117 days and that with naive T cells (CD4/CD45RA) at a median of 188 days posttransplantation. Our findings suggest that allogeneic transplantation from a matched family donor for nonmalignant disorders can be successfully performed using high doses of CD34 cells, moderate T cell depletion, and no posttransplantation immunosuppression.

摘要

为了消除移植物抗宿主病(GVHD)的有害影响,对非恶性疾病进行异基因移植时采用了高剂量CD34细胞输注、部分T细胞清除且不进行移植后GVHD预防。1998年至2004年期间,对16例有匹配相关供者的患者进行了治疗。中位年龄为1.5岁(范围为5个月至18岁)。预处理方案包括白消安16mg/kg、环磷酰胺200mg/kg、抗胸腺细胞球蛋白(ATG)25mg/kg和氟达拉滨200mg/m²。未给予GVHD预防措施。通过免疫磁珠阳性选择的高剂量CD34细胞以中位剂量10.7×10⁶ CD34/kg(范围为7.4 - 50×10⁶)进行输注。共给予1×10⁵/kg T细胞。所有患者均实现植入,无移植排斥反应。移植后中位37个月(范围为18 - 89个月)时,所有患者均存活且状况良好。仅1例患者发生慢性GVHD。移植期间及移植后未发生严重感染事件。移植后中位117天时观察到CD3/CD4 T细胞>200/μL的免疫重建,中位188天时观察到初始T细胞(CD4/CD45RA)的免疫重建。我们的研究结果表明,对于非恶性疾病,使用高剂量CD34细胞、适度T细胞清除且不进行移植后免疫抑制,可成功进行来自匹配家族供者的异基因移植。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验